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Chestnut (horse color)

Chestnut is a hair coat color of horses consisting of a reddish-to-brown coat with a mane and tail the same or lighter in color than the coat. Chestnut is characterized by the absolute absence of true black hairs. It is one of the most common horse coat colors, seen in almost every breed of horse.

Chestnut is a very common coat color but the wide range of shades can cause confusion. The lightest chestnuts may be mistaken for palominos, while the darkest shades can be so dark they appear black. Chestnuts have dark brown eyes and black skin, and typically are some shade of red or reddish brown. The mane, tail, and legs may be lighter or darker than the body coat, but unlike the bay they are never truly black. Like any other color of horse, chestnuts may have pink skin with white hair where there are white markings, and if such white markings include one or both eyes, the eyes may be blue. Chestnut foals may be born with pinkish skin, which darkens shortly afterwards.[1][better source needed]

Chestnut is produced by a recessive gene. Unlike many coat colors, chestnut can be true-breeding; that is, assuming they carry no recessive modifiers like pearl or mushroom, the mating between two chestnuts will produce chestnut offspring every time. This can be seen in breeds such as the Suffolk Punch and Haflinger, which are exclusively chestnut. Other breeds including the American Belgian Draft and Budyonny are predominantly chestnut. However, a chestnut horse need not have two chestnut parents. This is especially apparent in breeds like the Friesian horse and Ariegeois pony which have been selected for many years to be uniformly black, but on rare occasions still produce chestnut foals.

Visual identification

A chestnut horse with white markings

Chestnuts can vary widely in shade and different terms are sometimes used to describe these shades, even though they are genetically indistinguishable. Collectively, these coat colors are usually called "red" by geneticists.

A liver chestnut
This light, flaxen, mealy chestnut Haflinger might be mistaken for a palomino

Chestnut family colors

Chestnut is considered a "base color" in the discussion of equine coat color genetics. Additional coat colors based on chestnut are often described in terms of their relationship to chestnut:

A red dun has a light reddish- tan body and dark red primitive markings and points

Combinations of multiple dilution genes do not always have consistent names. For example, "dunalinos" are chestnuts with both the dun gene and one copy of the cream gene.

Chestnut mimics

Bay horses have a red body but black "points"

Inheritance and expression

A young chestnut foal, showing slight lightening of skin, possibly related to the pheomelaninistic characteristics of chestnut genetics. The skin will darken as the foal becomes older. Skin depigmentation is not always seen in chestnut foals.
A chestnut foal with body-clipped head and neck, showing two-toned hair shaft, lighter at the roots

The chestnut or sorrel color, genetically considered "red", is caused by one of two recessive alleles at the extension locus (genetics). Extension has three known alleles: the wildtype "E", necessary for the bay and black coat colors, plus two mutations "e" and "ea", both of which are capable of causing the chestnut color. Each individual horse has two copies of the extension gene. If either copy is "E", then the horse will be bay- or black-based. But if the two copies are any combination of "e" and "ea" (e/e, e/ea, or ea/ea), then the horse will be red-based. Alternate extension "ea" is rare and there is no known difference in appearance between it and the more common "e".[5][6]

Because the red color is recessive, two bay or black parents can produce a chestnut foal if both carry "e" or "ea". However, two chestnut parents cannot produce a bay or black foal.

The extension locus (genetics) is found on chromosome 3 (ECA3) and is part of the gene that codes for the equine melanocortin 1 receptor (MC1R). This receptor is part of a signalling pathway which when activated causes melanocytes to produce eumelanin, or black pigment, instead of pheomelanin, or red pigment.[7] The two mutant alleles "e" and "ea" code for dysfunctional receptors unable to activate this pathway, so absent "E", only red pigment can be produced. At least one copy of the functional "E" allele is required to activate the signal and produce black pigment. In general, alleles that create fully functional MC1R proteins are inherited dominantly and result in a black-based coat color ("E"), while mutated alleles that create "dysfunctional" MC1R are recessive and result in a lighter coat color ("e").

Normally MC1R would bind to the Melanocyte-stimulating hormone (MSH) which is released by the pituitary gland[7] and stimulates the production and release of melanin in skin and hair. Red hair color in horses ("e") is created by a missense mutation in the code for MC1R,[8] which results in a protein that cannot bind to MSH. When only mutant copies ("e) of the gene are available, non-functional MC1R proteins are produced. As a result, no black pigment is deposited into the hair and the entire coat is red-based. However, the skin of chestnut horses is still generally black, unless affected by other genes. Some chestnut foals are also born with lighter eyes and lightened skin, which darken not long after birth. This is not the same as the blue eyes and pink skin seen at birth in foals carrying the champagne gene. It is a genetic mechanism not fully understood, but may be related to the pheomelanistic characteristics of "e".

Though "E" allows the production of black pigment, it can also allow for red pigment in some parts of the animal as seen in bay horses. This happens when it is locally antagonized by the agouti signalling peptide (ASIP), or agouti gene, which "suppresses" black color and allows some red pigment to be formed.

See also

References

  1. ^ "Foal Colors". Retrieved November 30, 2021.
  2. ^ "General Glossary". American Quarter Horse Association. Archived from the original on July 7, 2011. Retrieved December 25, 2010.
  3. ^ Henner, J; PA Poncet; L Aebi; C Hagger; G Stranzinger; S Rieder (August 2002). "Horse breeding: genetic tests for the coat colors chestnut, bay and black. Results from a preliminary study in the Swiss Freiberger horse breed". Schweizer Archiv für Tierheilkunde. 144 (8): 405–412. doi:10.1024/0036-7281.144.8.405. The statistical analysis of 1369 offspring from five stallions indicate, that darker shades of basic color phenotypes (dark chestnut, dark bay) follow a recessive mode of inheritance in the Franches-Montagnes horse breed.
  4. ^ Locke, MM; LS Ruth; LV Millon; MCT Penedo; JC Murray; AT Bowling (2001). "The cream dilution gene, responsible for the palomino and buckskin coat colors, mapes to horse chromosome 21". Animal Genetics. 32 (6): 340–343. doi:10.1046/j.1365-2052.2001.00806.x. PMID 11736803. The eyes and skin of palominos and buckskins are often slightly lighter than their non-dilute equivalents.
  5. ^ "Red Factor". UC Davis Veterinary Genetics Laboratory. Retrieved October 5, 2023.
  6. ^ Wagner, H-J; Reissmann, M. (2000). "New polymorphism detected in the horse MC1R gene". Animal Genetics. 31 (4): 289–290. doi:10.1046/j.1365-2052.2000.00655.x. PMID 11086549. Within the tested chestnut coloured horse population, no association between both alleles e respectively ea and one of the variable chestnut phenotypes could be observed. Different individuals regarding to the shade of their chestnut coat colour were found in every group of the genotypes (e/e), (e/ea) and (ea/ea).
  7. ^ a b Online Mendelian Inheritance in Man (OMIM): MELANOCORTIN 1 RECEPTOR; MC1R - 155555
  8. ^ Marklund, L.; M. Johansson Moller; K. Sandberg; L. Andersson (1996). "A missense mutation in the gene for melanocyte-stimulating hormone receptor (MC1R) is associated with the chestnut coat color in horses". Mammalian Genome. 7 (12): 895–899. doi:10.1007/s003359900264. PMID 8995760. S2CID 29095360.

Further reading

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